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rs9341266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9341266(C;T)
Make rs9341266(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position38068851
GeneCYP1B1, LOC107985872
is asnp
is mentioned by
dbSNPrs9341266
dbSNP (old)rs9341266
ClinGenrs9341266
ebirs9341266
HLIrs9341266
Exacrs9341266
Varsomers9341266
Maprs9341266
PheGenIrs9341266
Biobankrs9341266
1000 genomesrs9341266
hgdprs9341266
ensemblrs9341266
gopubmedrs9341266
geneviewrs9341266
scholarrs9341266
googlers9341266
pharmgkbrs9341266
gwascentralrs9341266
openSNPrs9341266
23andMers9341266
23andMe allrs9341266
SNP Nexus

SNPshotrs9341266
SNPdbers9341266
MSV3drs9341266
GWAS Ctlgrs9341266
GMAF0.05188
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19293312OA-icon.png] Association of CYP1B1 haplotypes and breast cancer risk in Caucasian women


[PMID 19015200OA-icon.png] Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer.


[PMID 19479063OA-icon.png] Phase I metabolic genes and risk of lung cancer: multiple polymorphisms and mRNA expression.


ClinVar
Risk rs9341266(T;T)
Alt rs9341266(T;T)
Reference Rs9341266(C;C)
Significance Probable-non-pathogenic
Disease Primary congenital glaucoma Peters anomaly
Variation info
Gene CYP1B1
CLNDBN Primary congenital glaucoma Peters anomaly
Reversed 1
HGVS NC_000002.11:g.38295994G>A
CLNSRC
CLNACC RCV000316656.1, RCV000373665.1,